FHIT c.348+20284T>C

Variant ID: 3-59887788-A-G

NM_002012.2(FHIT):c.348+20284T>C

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Genome-wide SNP typing reveals signatures of population history.

Genomics
Hughes, Austin L AL; Welch, Robert R; Puri, Vinita V; Matthews, Casey C; Haque, Kashif K; Chanock, Stephen J SJ; Yeager, Meredith M
Publication Date: 2008-07

Variant appearance in text: rs294451
PubMed Link: 18485661
Variant Present in the following documents:
  • Main text
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